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Mom has AD and husband abandoned her.
I am writing this because I don’t know where else to turn and I’m hoping somebody out there has gone through something similar. My mother and stepfather have been married for 21 years and I’ve had a pretty happy marriage. My stepfather came down with Parkinson’s a few years ago and is in the later stages now and in an AL…
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Working through the issues (and emotions) - giving and requesting ideas for help
Hi. I just joined this group and have reviewed a number of strings. I find it crazy that with as rampant as this disease is, each case is still somewhat unique and there is not one methodology to deal with all cases. I look forward to learning from you all! I want to ask for direction as well as share some things that our…
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Ok - Need advice and suggestions multiple languages
I’ve become my mom’s full time care taker a few months ago. I sold my house, remodeled their basement and moved in to stay with her. My mom was my best friend we had fun together and did mostly everything together. She is 78 and we’ve been fighting this crappy disease for 4 years; unfortunately she is getting worse.…
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New here, are there any books aimed at the person who has dementia?
Hello, I had the slum test and was found to me on the border of mci and dementia. Thyroid test and b12 test came back normal range. Waiting on diabetes and will have an MRI on Friday. I am wondering if there any books you can recommend that are directed towards the patient and not necessarily the caregiver. I found a lot…
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How do I get my sister to the doctor?
Hi, I am new to the forum. I am sure this question has been asked by many people that are starting this journey. My sister thinks she is fine and ignores our requests to have her make an appointment to see a doctor. We know that she is not managing her finances properly and is making very poor decisions and possibly making…
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It Begins
After my fathers inital diagnosis little while ago without a tear; today it hit me hard. A distant friend that my parents visited (with prior warning of the situation), spoke of how different my dad was generally and how in ~5yrs since last seeing both my parents the changes in my dad. Denial - for the longest time we've…
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looking for some hearts and souls that understand
Hello Dear Community, Dad and I went to a neurologist appointment today to get him established with someone here after his move closer to me. You all have supported me through so much already. I thank you. It was our first time out together since his move here in late June. It was good to be out with him. I was so nervous…
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Long vent, sorry in advance...
In 2021 my grandparents moved my great aunt into the same apartment complex as me, less than a year after my mother passed away suddenly (and without warning) back in 2020. I was instantly forced into caring for my aunt without any sort of discussion. So now I am 35 and am currently the main caretaker for my 94 year old…
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Support for the spouses or partners of dementia caregivers!
:/ Is there any information on support groups for the spouses or partners or the caregivers or info on what it can do to a relationship or marriage? Any information is greatly appreciated!
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We need help!
My husband and his siblings are struggling to get their mother into assisted living. Doctors have been ZERO help with diagnoses and claim she has memory loss due to old age. She has presented well at her last 2 appointments. However we get 5-10 calls daily because of numerous things. (Lost her keys, lost her purse, cant…
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In home help
Tomorrow I will be talking with an agency that will provide in home help for my DH so I can do so many needed things that I have been putting on hold since his diagnosis in January. I have been utilizing family and friends to spend time with him when i have appts or do something socially, but some of his needs are more…
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How to become a provider for my Dad
This is a long story short. New to this. Dad has Dementia pretty bad and wife kicked him out 2 weeks ago. Us kids have been trying to care but super hard with this new lifestyle for him. The other day he fell at my sister's and we were in the ER for 2 days. He was transferred to a rehabilitation facility. He hates it. I…
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Father in law early stages , and visiting him soon
Hi everyone! So glad I found this website right now. What a relief wow. Story goes , my husband went to visit his parents in a different state last week. When he arrived, his brother pulled him aside and told him there father is starting to forget things, ask where he is, fighting with his wife and more. Side note : My…
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Working with an uncooperative caregiver/parent
My dad is the primary caregiver of my mom. My mom is in the middle stages of Alzheimer's and they are living alone in their own home. Dad refuses to share medical information regarding mom or himself (my siblings and I have seen a decline in his cognition, behaviors and abilities). Dad is unable to speak due to Aphasia,…
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New Here: Looking for support/community for "secondary" caregivers, extended family
Hi Everyone. My first time here. My sister in law was diagnosed with early on-set Alz about 16 months ago (after about 4 years of misunderstood difficulties) and seems to be progressing very quickly. I'm with her at least two days a week as a secondary caregiver to 1) spend time with her and 2) help take some of the…
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Navigating Family Dynamics: Post removed
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Questionnaire d'enquête
Bonjour à tous, J'effectue une enquête dans le cadre de ma formation qui porte sur "La nutrition peut-elle améliorer les troubles cognitifs dans la maladie d'Alzheimer et les maladies apparentées ?" et j'aurai besoin du témoignage de personnes touchées par cette maladie neurodégénérative ou les aidants d'une personne…
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New here, need advice
Hello everyone, Im new here. I was recommended this site after I posted for help on reddit. My mother is going to be diagnosed tomorrow with Alzheimer's. I've seen the signs in her for a while now, but have been putting off the inevitable. Alzheimer's runs in our family. Her mother passed from it, her brother is starting…
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Tone Deaf Invitation
A couple with whom DH and I have been close friends for 40 plus years just invited ME to a small dinner party celebrating the wife's 80th birthday. The invitation spelled out that I should get one of my children to watch my DH and just come by myself. I am miffed and maybe even insulted by this request. Has this happened…
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ALSP support group
My mom was DX with ALSP it’s a rare/genetic for of Alzheimer.. I was wondering if there was any type of support groups even virtual support groups that anybody has or has gone through that could help me. I love to join a support group, but I don’t know where to start, Can guide me?
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Being trans and caring for someone with Alzheimer's
Hey all, I am new here and looking for some type of support, but am unsure if this is the right place? I am a transgender person early-ish in my transition and my grandmother/best friend has been diagnosed with alzheimer's for around 2 years now. As my transition has progressed, so have her symptoms. Some of my family has…
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How to have DH let family and friends know of his diagnosis
Hi, I"m new here (although did use this site often when helping with my Mom who passed from Alz). THis time my DH has been diagnosed with demientia - though we haven't narrowed it down to a specific type yet. SO still early on. MY DH is still in denial or hoping something will "fix" the mild(his perception) issues he's…
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Mom had dementia, now dad has it.
Hi, my mom passed on about 6 years ago after dealing with early onset Alzheimer's. Now my dad has been diagnosed with it, and I just came here for some support because, although he's not in the advanced stages yet, I'm starting to see changes in his memory. It reminds me of what my mom went through and how I felt when she…
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The ups and downs of family dynamics
Wowow , where do I start , for one I am grateful for this forum/service for us sandwich generation families we are going through this storm (analogy ofcourse ) for my situation mom was diagnosed 6-8 months ago , but with not a clear diagnosis , but nevertheless things have become like a storm gathering steam , that's how…
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To correct or not....?
I am new to the support community. My mother was diagnosed with Alzheimer's in 2022. She is now in an Assisted Living near me. She is always wanting to have these deep conversations with me about her living situation but never really comprehends what I tell her. She keeps referring to the Assisted living as "school" and…
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Family Giving Me Conflicting Advice
Hi everyone! I (25) am the main caretaker for my mother (59) who was diagnosed with Alzheimer's back in 2022. Recently we've noticed some progression, she recently forgot my name for the first time so it's kicked my brain in to focusing on things like a will and POA. I was talking to my aunt the other night asking her…
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Grandpa’s phone calls
Hi everyone, I’m new here and seeking some advice. I have just recently learned that my grandpa has dementia. He still lives independently and I was unaware of his condition until now because my uncle didn’t tell me — all of my conversations with him had seemed normal until this weekend. For the past few days, he has been…
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Planning a Family Forum
Hi, everyone. I am in charge of planning a support group for resident's families, but I have been working in memory care for only about 5 months now. Yes, I have learned a lot about dementia and Alzheimer's and have a range of topics I would like to talk about at this family forum, but I would love to hear what other…
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Mom thinks she still works - she doesn't.
First- THANK YOU for any response. I am the eldest daughter, and my father is the primary caregiver of my Mom who has been officially diagnosed with Amnestic MCI (doc suspects we are heading into early stage AD.) Mom is starting a new trend of getting ready for work each morning and telling my Dad that she is going into…
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Wanting to go home
Hello, My mom was diagnosed with ALZ a year ago. Due to her diagnosis, we relocated her to a memory care center. The center is very nice and has many amenities and I visit weekly. She is high functioning and able to take care of many ADLs herself. She constantly talks about moving home which is unfortunately not an option…